R&D - CSO - Clinical Supply Chain Study Leader - BJ

ABOUT THE ROLE

As part of the Sanofi Research & Development organization, Clinical Supply Chain Operation (CSCO) and especially Clinical Supply Chain Project Management (CSC-PM) ensure that supplies needed to conduct any Sanofi Pharma and Vaccines clinical trial are set up, planned, ordered, packed and delivered in more than 80 countries for so that trial implementation is not disrupted.

CSC-PM is supporting the entire portfolio by designing, planning, executing, and monitoring supply chain activities in a timely and cost-effective manner and act as a critical asset in more than 300 on-going clinical trials.

As part of the CSC-PM team, the Clinical Supply Chain Study Leader (CSC-SL) coordinates overall CSCO operations of the entire clinical study including study planning, resource management, regulatory practices, policy adherence and contract research organization management (when applicable).

The CSC-SL will report to the CSC Group Head.

Main responsibilities :

• Clinical Study Management: accountable for operational management of clinical supplies in clinical trials ensuring timely delivery, budget adherence and compliance with GxPs, SOPs and Standards. The CSC Study leader is also accountable for problem solving, ensuring the best and more robust mitigation plan is identified and implemented.

• Team Coordination: responsible for coordinating the CSCO team to execute clinical supply study activities and collaborating with Clinical Supply Optimization Specialist (CSOS) for optimal supply chain system settings.

• Strategy and communication: Develops and communicates the best strategy for study supply in the study team, leading Operational Supply Meetings and revising strategies as needed.

• Key liaison: Serves as the primary contact for the Global Study Manager (GSM) and participated in the Core Study Team as the leader and expert for clinical supply activities.

• Documentation and local team support: Collects, reviews, synthetizes study documentation, prepares study related materials, coordinates device sourcing strategy and supports local teams for site initiation.

About you

• Experience: 2+ years’ experience in pharmaceutical business required

• Soft skills: Listening, Conflict resolution, critical thinking, interpersonal skills

• Technical skills: Leadership, project management, organizational skills, strong communication (oral and written), negotiation, results oriented and decision making

• Education: Master degree of Science (BS) in Health Science or related discipline

• Languages: FR & EN

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

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